A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21032



Internal ID15827163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24474626..24481939hg38UCSC Ensembl
Outerchr15:24474194..24482500hg38UCSC Ensembl
Innerchr15:24719773..24727086hg19UCSC Ensembl
Outerchr15:24719341..24727647hg19UCSC Ensembl
Innerchr15:22270866..22278179hg18UCSC Ensembl
Outerchr15:22270434..22278740hg18UCSC Ensembl
Innerchr15:22270866..22278179hg17UCSC Ensembl
Outerchr15:22270434..22278740hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg388307
hg198307
hg188307
hg178307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA07029
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv21032
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer